BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    CAMPY THIOGLYCOLLATE (TUBE)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    S8 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    PROPAQ ENCORE MODELS 202, 204, 206; PROPAQ CS MODELS 242, 244, 246

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DENALI FEMORAL SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·April 18, 2014

    DA+ C SERIES SR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·October 31, 2012

    PLM A+3 MEDNET WRLSS

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·August 17, 2010